Drive

FDA UDI

Class II (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name: DRIVE FDA UDI
Generic Name: Bed mattress/cover set FDA UDI
Device Name: Pressure Prevention Retail Foam Product Description Bed Wedge 23"x23"x10",1EA,4/CS FDA UDI
Model / Reference: 0-67583 FDA UDI
Description: Pressure Prevention Retail Foam Product Description Bed Wedge 23"x23"x10",1EA,4/CS FDA UDI

Identifiers

Primary DI / UDI-DI: 00822383255286 FDA UDI
FDA Product Code: FNL FDA UDI
GMDN Term: Bed mattress/cover set FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5100 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Bed mattress/cover set

Drive by Drive Devilbiss Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Drive Devilbiss Healthcare

Sources (1)

FDA UDI 353a1c73-9051-45b0-a59d-5eb114e5fc79 33 fields · synced Jun 8, 2026